A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569365



Internal ID16356774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49252812..49265736hg38UCSC Ensembl
Innerchr15:49545009..49557933hg19UCSC Ensembl
Innerchr15:47332301..47345225hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3812925
hg1912925
hg1812925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4521n54
Supporting Variantsnssv842834, nssv842835, nssv842832, nssv842831, nssv842833, nssv842830
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569365
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer